Evidence map›Paper›PMID 42538965›Full record

ArticlebioRxiv : the preprint server for biology2026

Early life adversity disrupts adult social reward motivation.

Margie C Stricklin, Judy E Nyakoa, Kevin M Mesape, Moushmi S Bhat, Siarra S Rolle, Debra A Bangasser, Amelia Cuarenta

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Margie C StricklinNeuroscience Institute, Georgia State University, Atlanta, GA, USA.
Judy E NyakoaNeuroscience Institute, Georgia State University, Atlanta, GA, USA.ORCID 0009-0007-0169-0233
Kevin M MesapeNeuroscience Institute, Georgia State University, Atlanta, GA, USA.ORCID 0009-0000-6228-6014
Moushmi S BhatNeuroscience Institute, Georgia State University, Atlanta, GA, USA.
Siarra S RolleNeuroscience Institute, Georgia State University, Atlanta, GA, USA.
Debra A BangasserNeuroscience Institute, Georgia State University, Atlanta, GA, USA.ORCID 0000-0003-2951-4921
Amelia CuarentaNeuroscience Institute, Georgia State University, Atlanta, GA, USA.ORCID 0000-0002-0570-749X

Funding

Delineating the epigenetic and neural mechanisms by which early life scarcity alters motivated behaviorR01DA056534 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI Debra A Bangasser, Mathieu Wimmer · 2022 to 2026
$3.2M
Sex Differences In Stress Inoculation Of Addiction-Like PhenotypesR01DA049837 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI BANGASSER, DEBRA A · 2020 to 2024
$3.1M
Early life pain and its modulation by socioenvironmental factors: Implications for substance misuseR34DA061483 · NIDA · GEORGIA STATE UNIVERSITY · PI BANGASSER, DEBRA A, MURPHY, ANNE Z · 2024 to 2025
$723k
Determining the effect of early resource scarcity on adolescent addiction-related behavior and cell-type specific transcriptionR21DA059966 · NIDA · GEORGIA STATE UNIVERSITY · PI BANGASSER, DEBRA A, REINER, BENJAMIN CHARLES · 2023 to 2024
$467k
Lasting effects of early resource scarcity on cortical astrocyte structure and functionR21DA062844 · NIDA · GEORGIA STATE UNIVERSITY · PI Debra A Bangasser, Javier E Stern · 2025 to 2026
$435k
Early resource scarcity effects on addiction-related behavior: a novel role for retrotransposons.R00DA060266 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Amelia Cuarenta · 2026 to 2026
$249k
Early resource scarcity effects on addiction-related behavior: a novel role for retrotransposons.K99DA060266 · NIDA · GEORGIA STATE UNIVERSITY · PI CUARENTA, AMELIA · 2024 to 2024
$158k
NIDA NIH HHS K99 DA060266NIDA NIH HHS R00 DA060266NIDA NIH HHS R01 DA049837NIDA NIH HHS R01 DA056534NIDA NIH HHS R21 DA059966NIDA NIH HHS R21 DA062844NIDA NIH HHS R34 DA061483
6 · The paper itself

Abstract

Early life adversity can produce persistent changes during development that increase vulnerability to neuropsychiatric disorders. Although disruptions in reward processing are widely recognized as a hallmark of these disorders, reward is not a single construct. Distinct forms of reward including social interaction and primary rewards such as food rely on overlapping but dissociable neural circuitry and may be differentially affected by adverse experiences. Here, we used a rodent model of neonatal predator odor exposure (POE) to determine how early life threat influences motivation for social and sucrose reward in adulthood using operant procedures. Neonatal POE reduced adult motivation for a social reinforcer during an operant social self-administration task, whereas motivation for a sucrose reinforcer was unchanged. However, we did find a significant difference in sucrose self-administration with POE females pressing more for sucrose than control females. These findings demonstrate that neonatal threat does not produce a generalized deficit in motivation but rather selectively alters motivation across distinct reward domains. Together, this work identifies social reward as a particularly vulnerable behavioral domain following early life threat and provides new insight into how adverse developmental experiences shape adult reward-related behavior.

Identifiers

PMID42538965
PMCPMC13419419

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.